Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thrive

被引:19
作者
Lamont, PJ
Thorburn, DR
Fabian, V
Vajsar, J
Hawkins, C
Saada, A
Durling, H
Laing, NG
Nevo, Y
机构
[1] Royal Perth Hosp, Neurogenet Unit, Dept Neurol, Perth, WA 6847, Australia
[2] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[4] Royal Perth Hosp, Dept Pathol, Perth, WA, Australia
[5] Univ Toronto, Hosp Sick Children, Div Neurol, Dept Paediat, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, Hosp Sick Children, Dept Lab Med, Toronto, ON M5G 1X8, Canada
[7] Shaare Zedek Med Ctr, Metab Dis Unit, Jerusalem, Israel
[8] Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Inst Child Dev, IL-69978 Tel Aviv, Israel
[9] Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Paediat Neurol Unit, IL-69978 Tel Aviv, Israel
关键词
complex I deficiency; nemaline rods; developmental delay;
D O I
10.1055/s-2004-821243
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Three infants are described who had nemaline rods on muscle biopsy and isolated deficiency of complex I of the respiratory chain on biochemical analysis. They all manifested failure to thrive from birth, and hypotonia and muscle weakness within the first three months of life. Different genetic defects leading to isolated complex I deficiency have been described associated with a variety of morphological changes on muscle biopsy, but rods have not been described. Nemaline rods have been secondary phenomena in a number of conditions, as well as being the primary abnormality in nemaline myopathy. However, the combination of nemaline rods and complex I deficiency is an association not previously reported.
引用
收藏
页码:302 / 306
页数:5
相关论文
共 15 条
[1]   NEMALINE STRUCTURES IN POLYMYOSITIS - A NONSPECIFIC PATHOLOGICAL REACTION OF SKELETAL MUSCLES [J].
CAPE, CA ;
JOHNSON, WW ;
PITNER, SE .
NEUROLOGY, 1970, 20 (05) :494-&
[2]   A CASE OF NEMALINE MYOPATHY WITH OPHTHALMOPLEGIA AND MITOCHONDRIAL ABNORMALITIES [J].
FUKUNAGA, H ;
OSAME, M ;
IGATA, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1980, 46 (02) :169-177
[3]   What's new in neuromuscular disorders? The congenital myopathies [J].
Jungbluth, H ;
Sewry, CA ;
Muntoni, F .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2003, 7 (01) :23-30
[4]   Respiratory chain complex I deficiency - An underdiagnosed energy generation disorder [J].
Kirby, DM ;
Crawford, M ;
Cleary, MA ;
Dahl, HHM ;
Dennett, X ;
Thorburn, DR .
NEUROLOGY, 1999, 52 (06) :1255-1264
[5]  
KIRBY DM, 2004, IN PRESS J CLIN INVE
[6]   MIXED NEMALINE-MITOCHONDRIAL MYOPATHY [J].
KORNFELD, M .
ACTA NEUROPATHOLOGICA, 1980, 51 (03) :185-189
[7]   Mitochondrial encephalomyopathies [J].
Oldfors, A ;
Tulinius, M .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2003, 62 (03) :217-227
[8]   CHANGES AT NEUROMUSCULAR-JUNCTIONS IN AFFECTED MUSCLES OF NEOSTIGMINE-TREATED RATS, TENOTOMIZED RATS AND A PATIENT WITH NEMALINE MYOPATHY [J].
OSAME, M ;
KAWABUCHI, M ;
IGATA, A ;
SUGITA, H .
ACTA HISTOCHEMICA ET CYTOCHEMICA, 1977, 10 (01) :70-80
[9]  
Oya Y, 2000, Rinsho Shinkeigaku, V40, P452
[10]   ADULT-ONSET OF NEMALINE MYOPATHY, ASSOCIATED WITH CORES AND ABNORMAL MITOCHONDRIA [J].
POURMAND, R ;
AZZARELLI, B .
MUSCLE & NERVE, 1994, 17 (10) :1218-1220